Canonical Allele Identifier: PA263034
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49956
ClinVar RCV Id: RCV000043223 RCV002298454
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gly1579Ser
CA020963
NM_000548.5:c.4735G>A